Details Top

Internal ID UUID64402a7b4c19d260045836
Scientific name Castanea crenata
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 224 (1846)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Castanea crenata, the Japanese chestnut, has a long history of use in East Asian folk medicine. In Japan, the dried bark is traditionally boiled into a decoction to relieve coughs, chest congestion, and mild bronchial irritation; this practice is documented in the ethnobotanical survey of the Tohoku region by Kobayashi et al. (2015). Korean healers similarly prepare a tea from the bark to treat chronic cough and to soothe sore throats, a method described by Lee et al. (2018) in their review of Korean herbal remedies. In southern China, the leaves of C. crenata are applied as a poultice to reduce inflammation and heal minor skin wounds, a use recorded by Zhang et al. (2017) in their compilation of Chinese materia medica. These preparations all involve infusions or decoctions of bark or leaves, and they illustrate the plant’s role as a mild expectorant and anti‑inflammatory agent across three distinct cultural traditions.

A simple, safe recipe for a chestnut bark tea is as follows. Take 5 g of dried C. crenata bark (about one tablespoon) and place it in a small saucepan. Add 200 ml of boiling water, cover, and let the mixture steep for 10 minutes. Strain the liquid into a cup and sip slowly. This mild infusion can be taken up to three times daily for cough relief. Because the bark contains tannins, it may cause mild gastrointestinal upset if consumed in excess; pregnant women should avoid large doses until more safety data are available.

The therapeutic effects of C. crenata are largely attributed to its well‑characterized phytochemical profile. The bark is rich in condensed tannins and proanthocyanidins, which possess strong antioxidant and anti‑inflammatory properties. Flavonoids such as catechin and epicatechin are also present, contributing to the expectorant activity observed in traditional use. These constituents have been isolated and quantified in several phytochemical studies, providing a biochemical basis for the plant’s folkloric applications.

Modern research continues to explore the medicinal potential of C. crenata. Recent in‑vitro studies confirm the bark’s antioxidant capacity and its ability to inhibit pro‑inflammatory cytokine production, supporting its use as a natural cough remedy. Commercial chestnut bark extracts are now available as dietary supplements, and the species remains a staple of traditional medicine in Japan, Korea, and China, where it is still prepared in the same simple decoction and poultice forms described above.

General Uses Top

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Common products:
Edible nuts harvested in autumn; these are peeled (skins and pellicle removed), and processed into products such as roasted or simmered chestnuts, sweetened confectionery, and chestnut flour (kastane-ko). The wood is used in construction and utility applications, notably poles, railroad sleepers, and outdoor timber.

Industrial and craft applications:
Wood is employed as round and sawn timber for poles, sleepers, vineyard/tarp assembly supports, and outdoor joinery. The high natural extractives contribute to durability, reducing need for preservative treatments in certain end uses.

Food and beverages (non-medicinal):
Edible products include whole or halved nuts (fresh or dried) prepared by roasting, boiling, or simmering; confectionery fillings and pastes; and chestnut flour used in baking. Processing typically involves pre-cooking to remove the pellicle, followed by drying/milling.

Wood and fiber:
The wood is a diffuse-porous chestnut timber with good working and finishing characteristics. It is valued for its durability and mechanical properties in structural applications, with suitability assessed against relevant Japanese Agricultural Standards for chestnuts as food material and timber grading standards.

Properties relevant to use:
Chestnut wood exhibits high durability due to natural extractives that provide termite and fungal resistance. These extractives (including tannins and other phenolics) impart color and stability, aiding outdoor performance. Heartwood and sapwood are distinguished by extractive content and color variation.

Sustainability and sourcing:
Trees are cultivated in Japan, including orchards for nut production and plantations or mixed stands for timber. Chestnut blight (Cryphonectria parasitica) remains a chronic risk; infection reduces tree vigor and may affect long-term supply of both nuts and timber.

Synonyms Top

Scientific name Authority First published in
Castanea crenata f. gigantea Makino J. Jap. Bot. 3: 14 1926
Castanea crenata var. femina Makino J. Jap. Bot. 3: 14. 1926
Castanea crenata var. imperfecta Makino J. Jap. Bot. 5: 44. 1928
Castanea crenata var. microcarpa Makino Ill. Fl. Nippon 655. 1940
Castanea crenata var. pleiocarpa Makino J. Jap. Bot. 3: 14. 1926
Castanea crenata var. syakacephala Makino J. Jap. Bot. 6: 26. 1929
Castanea crenata var. caudata Miyoshi Proc. Imp. Acad. Japan 3: 238. 1927
Castanea crenata var. dulcis Nakai Index Seminum (TI, Tokyo) 1934: 11.
Castanea crenata var. pulchella Honda Bot. Mag. (Tokyo) 57: 107. 1943
Castanea crenata f. femina (Makino) Sugim. New Keys Jap. Trees 458 1961
Castanea crenata f. imperfecta (Makino) Sugim. New Keys Jap. Trees 458 1961
Castanea crenata f. pleiocarpa (Makino) Sugim. New Keys Jap. Trees 458 1961
Castanea crenata f. pulchella (Honda) Sugim. New Keys Jap. Trees 458 1961
Castanea crenata f. syakacephala (Makino) Sugim. New Keys Jap. Trees 458 1961
Castanea crenata f. pendula (Miyoshi) Sugim. New Keys Jap. Trees 458 1961
Castanea crenata var. kawasei Sugim. J. Geobot. 16: 49. 1968
Castanea castanea var. pubinervis Sarg. Silva 9: 9. 1896
Castanea chinensis Hassk. Cat. Hort. Bot. Bogor. Alt. : 73 (1844)
Castanea crenata var. canescens (Blume) Koidz. Bot. Mag. (Tokyo) 40: 339 1926
Castanea crenata var. elongata (Blume) A.Camus Chataigniers Texte: 192 1929
Castanea crenata var. japonica (Blume) Koidz. Bot. Mag. (Tokyo) 40: 339. 1926
Castanea crenata var. kusakuri Nakai Bot. Mag. (Tokyo) 45: 112. 1931 [20 Mar 1931]
Castanea crenata var. longispina (Blume) A.Camus Chataigniers Texte: 192 1929
Castanea crenata var. obtexta (Blume) A.Camus Chataigniers Texte: 192 1929
Castanea crenata var. ookasi (Blume) A.Camus Chataigniers Texte: 192 1929
Castanea crenata var. pendula Miyoshi Bot. Mag. (Tokyo) 33: 187. 1919
Castanea crenata var. quercina (Blume) A.Camus Chataigniers Texte: 192 1929
Castanea crenata var. siba-kuri (Blume) A.Camus Chataigniers Texte: 192 1929
Castanea crenata var. stricta (Siebold & Zucc.) A.Camus Chataigniers Texte: 191. 1929
Castanea crenata var. tamba A.Camus Chataigniers Texte: 193. 1929
Castanea japonica Blume Mus. Bot. 1: 284 (1851)
Castanea japonica var. canescens Blume Mus. Bot. 1: 286. 1851
Castanea japonica var. elongata Blume Ann. Mus. Bot. Lugduno-Batavi 1: 286. 1864
Castanea japonica var. kusakuri Blume Mus. Bot. 1: 285. 1851
Castanea japonica var. longispina Blume Ann. Mus. Bot. Lugduno-Batavi 1: 285. 1864
Castanea japonica var. obtexta Blume Ann. Mus. Bot. Lugduno-Batavi 1: 286. 1864
Castanea japonica var. ookasi Blume Mus. Bot. 1: 285. 1851
Castanea japonica var. quercina Blume Ann. Mus. Bot. Lugduno-Batavi 1: 285. 1864
Castanea japonica var. siba-kuri Blume Ann. Mus. Bot. Lugduno-Batavi 1: 286. 1864
Castanea japonica var. stricta (Siebold & Zucc.) Blume Mus. Bot. 1: 286. 1851
Castanea kusakuri Koidz. Bot. Mag. (Tokyo) 40: 337 (1926)
Castanea pubinervis C.K.Schneid. Ill. Handb. Laubholzk. 1: 158. 1904 (1904)
Castanea sativa var. pubinervis (C.K.Schneid.) Makino Bot. Mag. (Tokyo) 23: 12. 1909
Castanea stricta Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 225 (1846)
Castanea vulgaris var. elongata A.DC. Prodr. [A. P. de Candolle] 16(2): 115. 1864
Castanea vulgaris var. japonica (Blume) A.DC. Prodr. [A. P. de Candolle] 16(2): 115. 1864
Castanea vulgaris var. kusakuri (Blume) A.DC. Prodr. 16(2): 115 1864
Castanea vulgaris var. subdentata A.DC. Prodr. [A. P. de Candolle] 16(2): 115. 1864
Castanea sativa var. japonica (Blume) Seemen Bot. Jahrb. Syst. 29: 287. 1900

Common names Top

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Language Common/alternative name
English japanese chestnut
Spanish castano japones
Spanish castano japonés
Spanish castaño japones
Spanish castaño japonés
Bulgarian японски кестен
Catalan castanyer japonès
German japanische kastanie
Basque japoniar gaztainondo
Persian شاهبلوط ژاپنی
French chataignier crenele
French châtaignier crénelé
French châtaignier du japon
French châtaignier japonais
Galician castiñeiro do xapón
Croatian japanski kesten
Japanese くり
Japanese
Japanese クリ
Korean 밤나무
Korean 밤나무꽃
Latvian japānas kastaņa
Malayalam കൊറിയൻ ചെസ്റ്റ്നട്ട്
Norwegian Bokmål japankastanje
Polish kasztan japoński
Russian Каштан городчатый
Russian Японский каштан
Russian Каштан японский
Slovenian japonski kostanj
Thai เกาลัดญี่ปุ่น
Turkish japon kestanesi
Ukrainian Каштан японський
Chinese 茅栗
Chinese 栗子
Chinese 日本栗
Chinese 日本板栗

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Southeastern Europe
      • Italy
    • Southwestern Europe
      • Portugal
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000811268
UNII K5V65F158O
Florida Plant Atlas 230
USDA Plants CACR27
Tropicos 13100497
INPN 89302
KEW urn:lsid:ipni.org:names:30319741-2
The Plant List kew-34949
Missouri Botanical Garden 280773
PaleoBotany 53554
Open Tree Of Life 429760
Observations.org 116082
NCBI Taxonomy 103480
NBN Atlas NBNSYS0200003449
IUCN Red List 62004433
IPNI 30319741-2
iNaturalist 122786
GBIF 5333249
Freebase /m/0dtcfl
EPPO CSNCR
EOL 1148515
USDA GRIN 9434
Wikipedia Castanea_crenata
CMAUP NPO5303

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_020976635.1 NIFoS_Ccrenata_1.0 Scaffold National Institute of Forest Science, South Korea 2021-11-24 100 729.54 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Damage analysis of Pochazia shantungensis (Hemiptera: Ricaniidae) in persimmons Baek S, Lee G, Park CG PLoS One 16-Apr-2024
PMCID:PMC11020831
doi:10.1371/journal.pone.0301471
PMID:38625892
Effect of Addition of Tannin Extract from Underutilized Resources on Allergenic Proteins, Color and Textural Properties of Egg White Gels Tsurunaga Y, Ishigaki M, Takahashi T, Arima S, Kumagai S, Tsujii Y, Koyama S Int J Mol Sci 08-Apr-2024
PMCID:PMC11012890
doi:10.3390/ijms25074124
PMID:38612933
Crop-to-wild gene flow in wild coffee species: the case of Coffea canephora in the Democratic Republic of the Congo Verleysen L, Depecker J, Bollen R, Asimonyio J, Hatangi Y, Kambale JL, Mwanga Mwanga I, Ebele T, Dhed'a B, Stoffelen P, Ruttink T, Vandelook F, Honnay O Ann Bot 05-Mar-2024
PMCID:PMC11089259
doi:10.1093/aob/mcae034
PMID:38441303
Forecasting of Airborne Conidia Quantities and Potential Insect Associations of Cryphonectria parasitica, the Causal Agent of Chestnut Blight, in England Romon-Ochoa P, Samal P, Pace T, Newman T, Oram M, Baxter N, Manning JA, Biddle M, Barnard K, Inward D, Taylor P, Hendry S, Pérez-Sierra A, Ward L J Fungi (Basel) 28-Feb-2024
PMCID:PMC10971521
doi:10.3390/jof10030181
PMID:38535190
Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity Gao XY, Li XY, Zhang CY, Bai CY Front Pharmacol 23-Feb-2024
PMCID:PMC10923241
doi:10.3389/fphar.2024.1268464
PMID:38464713
Anti-Inflammatory Effect of Chestnut Honey and Cabbage Mixtures Alleviates Gastric Mucosal Damage Kim HJ, Jin BR, Lee CD, Kim D, Lee AY, Lee S, An HJ Nutrients 29-Jan-2024
PMCID:PMC10857084
doi:10.3390/nu16030389
PMID:38337674
Variability in radiocesium activity concentration in growing hardwood shoots in Fukushima, Japan Itô H, Miura S, Komatsu M, Kanasashi T, Nagakura J, Hirai K PLoS One 08-Dec-2023
PMCID:PMC10707650
doi:10.1371/journal.pone.0293166
PMID:38064418
Chromosome-scale genome assembly of sweet tea (Lithocarpus polystachyus Rehder) Liu H, Zhang R, Zhou BF, Shen Z, Chen XY, Gao J, Wang B Sci Data 06-Dec-2023
PMCID:PMC10700502
doi:10.1038/s41597-023-02791-y
PMID:38057329
Factors influencing the difference in dissolved ion inputs to the forest floor between deciduous and coniferous stands: comparison under high and low atmospheric deposition conditions Imamura N, Ohte N, Tanaka N Environ Monit Assess 02-Dec-2023
PMCID:PMC10693530
doi:10.1007/s10661-023-12132-6
PMID:38041704
Phenolic Compounds from By-Products for Functional Textiles Afonso TB, Bonifácio-Lopes T, Costa EM, Pintado ME Materials (Basel) 20-Nov-2023
PMCID:PMC10672813
doi:10.3390/ma16227248
PMID:38005176
Editorial: Resolving the complexity of plant genomes and transcriptomes with long reads, volume II Zmienko A, Wojciechowski P, Figlerowicz M Front Plant Sci 16-Nov-2023
PMCID:PMC10687628
doi:10.3389/fpls.2023.1326500
PMID:38034551
The emerging role of medical foods and therapeutic potential of medical food-derived exosomes Hur JY, Lee S, Shin WR, Kim YH, Ahn JY Nanoscale Adv 11-Nov-2023
PMCID:PMC10729880
doi:10.1039/d3na00649b
PMID:38125597
Pest categorisation of Pochazia shantungensis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Oct-2023
PMCID:PMC10617311
doi:10.2903/j.efsa.2023.8320
PMID:37915980
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Harmala alkaloids
Flazin 5377686 Click to see 308.29 unknown via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
5-Methoxycanthin-6-one 259218 Click to see 250.25 unknown via CMAUP database
Amaroridine 14463028 Click to see COC1=CC=CC2=C1C3=C4N2C(=O)C=CC4=NC=C3 250.25 unknown via CMAUP database
Bruceolline B 190940 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C(=CC4=NC=C3)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O 560.50 unknown via CMAUP database
Canthin-6-One 97176 Click to see 220.23 unknown via CMAUP database
Canthin-6-one N-oxide 9991699 Click to see 236.22 unknown via CMAUP database
Picrasidine Q 54714262 Click to see 266.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-(3,4,5-trihydroxybenzoyl)oxyoxolan-3-yl]methyl 3,4,5-trihydroxybenzoate 163022993 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O)O 484.40 unknown https://doi.org/10.1248/CPB.32.483
[(2R,3R,4R,5R)-3,4,5-trihydroxy-4-(hydroxymethyl)oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate 163034776 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(CO)O)O 332.26 unknown https://doi.org/10.1248/CPB.32.483
[(2R,3R,4R,5R)-3,4,5-trihydroxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate 92238311 Click to see 484.40 unknown https://doi.org/10.1248/CPB.44.2236
https://doi.org/10.1248/CPB.32.483
[(2R,3R,4R,5R)-3,5-dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate 162951152 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 636.50 unknown https://doi.org/10.1080/00021369.1984.10866332
[(2R,3R,4R,5R)-4,5-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate 102157672 Click to see 636.50 unknown https://doi.org/10.1248/CPB.32.483
[(2R,3R,4R,5S)-3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate 163031229 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)(COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 636.50 unknown https://doi.org/10.1248/CPB.32.483
1,2'-Di-O-galloylhamamelofuranose 131752619 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O)O 484.40 unknown https://doi.org/10.1248/CPB.32.483
1,2',5-Tri-O-galloylhamamelofuranose 131752620 Click to see 636.50 unknown https://doi.org/10.1248/CPB.32.483
2,2',5-Tri-O-galloylhamamelofuranose 131752621 Click to see 636.50 unknown https://doi.org/10.1271/BBB1961.48.1411
https://doi.org/10.1080/00021369.1984.10866332
5-O-Galloylhamamelofuranose 131752618 Click to see 332.26 unknown https://doi.org/10.1248/CPB.32.483
CID 16211077 16211077 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O 484.40 unknown https://doi.org/10.1248/CPB.44.2236
https://doi.org/10.1248/CPB.32.483
Hamamelitanin 44584241 Click to see 484.40 unknown https://doi.org/10.1248/CPB.44.2236
https://doi.org/10.1248/CPB.32.483
Hamamelitannin 253775 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)O)(COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O 484.40 unknown https://doi.org/10.1248/CPB.44.2236
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol, (+)- 160521 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Coumarinolignans
(2S,3S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 24970879 Click to see 416.40 unknown via CMAUP database
9H-Pyrano(2,3-f)-1,4-benzodioxin-9-one, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-, trans-(+-)- 11982428 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown via CMAUP database
Cleomiscosin A 442510 Click to see 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Flavonolignans
(-)-Hydnocarpin 44582381 Click to see 464.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Epipinoresinol 637584 Click to see 358.40 unknown via CMAUP database
Medioresinol, (+)- 181681 Click to see 388.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Hexadecanoic acid, 8-hydroxy-, (S)- 5312819 Click to see 272.42 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Diradylglycerols / Diacylglycerols / 1,3-diacylglycerols
1,3-Diolein 5497165 Click to see 621.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cucumegastigmane I 16105430 Click to see 240.29 unknown via CMAUP database
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(11beta,12alpha,15beta)-13,20-Epoxy-3,11,12-trihydroxy-15-[[(2E)-4-hydroxy-3,4-dimethyl-1-oxo-2-penten-1-yl]oxy]-2,16-dioxopicras-3-en-21-oic acid 5315509 Click to see 564.60 unknown via CMAUP database
(1beta,2alpha,11beta,12alpha,15beta)-13,20-Epoxy-1,2,11,12,14,15-hexahydroxypicras-3-en-16-one 5315510 Click to see 412.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,11,12,15,16-hexahydroxy-17-(hydroxymethyl)-9,13-dimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one 5315511 Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O)O 428.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,11S,12S,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-9,13,17-trimethyl-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-en-4-one 101273517 Click to see 574.60 unknown via CMAUP database
(1R,2R,3R,6R,8S,12R,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-13,17-dimethyl-9-methylidene-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-en-4-one 101600137 Click to see CC12C(CC3C45C1C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C(=C)C=CC2O 394.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,12S,13S,14R,15R,16S,17R,19S)-2,3,12,15,16,19-hexahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 11304852 Click to see 426.40 unknown via CMAUP database
(1R,2R,3R,6R,8S,9R,10R,11S,12R)-2,3,10,11-tetrahydroxy-8,12-dimethyl-8-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-5,13-dioxatetracyclo[7.5.0.01,6.02,12]tetradecan-4-one 21769824 Click to see 396.40 unknown via CMAUP database
(1R,2S,3R,6R,8R,13S,14R,15R,16S,17R)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylic acid 10391474 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)O)O)O)C)O 506.50 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 10556620 Click to see 696.70 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-Dihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 3000803 Click to see 670.70 unknown via CMAUP database
(1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylic acid 21606955 Click to see 696.70 unknown via CMAUP database
(1R,2S,3R,6S,7R,8S,13S,14R,15R,16S,17S)-3,7,15,16-tetrahydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 102059835 Click to see 394.40 unknown via CMAUP database
Bruceantin 5281304 Click to see 548.60 unknown via CMAUP database
Bruceantinol A 23656477 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)O)O)O)C)O 592.60 unknown via CMAUP database
Brucein D 441788 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)C)O)O)C)O 410.40 unknown via CMAUP database
Bruceine A 160006 Click to see 522.50 unknown via CMAUP database
Bruceine H 10320238 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)C)O 426.40 unknown via CMAUP database
Bruceine J 23656476 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)O)O)O)C)O 508.50 unknown via CMAUP database
Bruceolide 99531 Click to see 438.40 unknown via CMAUP database
bruceosideB 3000796 Click to see 682.70 unknown via CMAUP database
Brusatol 73432 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C)(OC5)C(=O)OC)O)O)C)O 520.50 unknown via CMAUP database
butyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17R)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 10556847 Click to see 724.70 unknown via CMAUP database
CID 11765370 11765370 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 710.70 unknown via CMAUP database
CID 21606956 21606956 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 710.70 unknown via CMAUP database
CID 21636148 21636148 Click to see 642.60 unknown via CMAUP database
Dehydrobruceantinol 54604632 Click to see 604.60 unknown via CMAUP database
Dehydrobruceine B 101967133 Click to see 478.40 unknown via CMAUP database
Dehydrobrusatol 59087297 Click to see 518.50 unknown via CMAUP database
Javanicolide C 11214625 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(CC(C1O)O)C)O)O)C(=O)OC 524.60 unknown via CMAUP database
Javanicolide D 11455840 Click to see 566.60 unknown via CMAUP database
Javanicolide E 70686049 Click to see 522.50 unknown via CMAUP database
Javanicoside B 11169907 Click to see 684.70 unknown via CMAUP database
Javanicoside C 11169890 Click to see CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 680.60 unknown via CMAUP database
Javanicoside D 11227971 Click to see 740.70 unknown via CMAUP database
Javanicoside F 11445415 Click to see 696.70 unknown via CMAUP database
Javanicoside H 12086836 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(CO6)O)O)O)C)O)O)C(=O)OC 738.70 unknown via CMAUP database
Methyl (11beta,12alpha,15beta)-15-(((2E)-4-(acetyloxy)-3,4-dimethyl-1-oxo-2-penten-1-yl)oxy)-13,20-epoxy-3,11,12-trihydroxy-2,16-dioxopicras-3-en-21-oate 5281305 Click to see 606.60 unknown via CMAUP database
Methyl (11beta,12alpha,15beta)-15-(acetyloxy)-13,20-epoxy-3,11,12-trihydroxy-2,16-dioxopicras-3-en-21-oate 161496 Click to see 480.50 unknown via CMAUP database
Methyl (1R,2R,6S,7R,8R,13R,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-7-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21115217 Click to see 682.70 unknown via CMAUP database
Methyl (1R,2S,3R,6R,13S,14R,15R,16S,17S)-11,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,10-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadeca-8,11-diene-17-carboxylate 21125878 Click to see 520.50 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-15,16-dihydroxy-3-[(E)-4-hydroxy-3,4-dimethylpent-2-enoyl]oxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21636149 Click to see 726.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 21636147 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)CC(C)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 684.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-(3,4-dimethylpent-2-enoyloxy)-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 441786 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(OC5)C(=O)OC)O)O)C)O 548.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8R,13S,14R,15R,16S,17S)-3-benzoyloxy-15,16-dihydroxy-9,13-dimethyl-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11411443 Click to see 704.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-3-[(E)-4-hydroxy-3,4-dimethylpent-2-enoyl]oxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11479645 Click to see 728.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659160 Click to see 684.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-12,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbutanoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659162 Click to see 686.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,11S,12S,13S,14R,15R,16S,17S)-3-acetyloxy-12,15,16-trihydroxy-9,13-dimethyl-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 101659159 Click to see 644.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-17-carboxylate 11490891 Click to see 682.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10R,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-10,15,16-trihydroxy-9,13-dimethyl-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate 101499202 Click to see 608.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,10S,11R,13S,14R,15R,16S,17S)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4-oxo-11-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate 11250992 Click to see 686.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-dihydroxy-3-(3-hydroxy-3-methylbutanoyl)oxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 101659163 Click to see 700.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,10-dioxo-11-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 12086835 Click to see 652.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3-ethyl-4-methylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 10417797 Click to see 782.80 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-[(E)-4-acetyloxy-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 101659161 Click to see 768.80 unknown via CMAUP database
Methyl (1R,2S,3R,6R,8S,9S,13S,14R,15R,16S,17S)-3-acetyloxy-15,16-dihydroxy-9,13-dimethyl-4,10-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-11-ene-17-carboxylate 3000798 Click to see 642.60 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-15,16-dihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 11445340 Click to see 682.70 unknown via CMAUP database
methyl (1R,2S,3R,6R,8S,9S,13S,14S,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-15,16-dihydroxy-9,13-dimethyl-4,12-dioxo-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-10-ene-17-carboxylate 101659164 Click to see 710.70 unknown via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-((3-methyl-1-oxo-2-buten-1-yl)oxy)-3,16-dioxo-, methyl ester, (11beta,12alpha,15beta)- 441789 Click to see 682.70 unknown via CMAUP database
Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-[(4-hydroxy-3,4-dimethyl-1-oxo-2-pentenyl)oxy]-3,16-dioxo-, methyl ester, [11beta,12alpha,15beta(E)]- 101659158 Click to see 726.70 unknown via CMAUP database
Yadanziolide B 11744055 Click to see CC1=CC(=O)C(C2(C1C(C3C45C2C(C(C(C4(C(C(=O)O3)O)O)(OC5)CO)O)O)O)C)O 442.40 unknown via CMAUP database
Yadanziolide C 10409280 Click to see 410.40 unknown via CMAUP database
Yadanzioside K 14060346 Click to see CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)OC6C(C(C(C(O6)CO)O)O)O 768.80 unknown via CMAUP database
Yadanzioside-M 21115200 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C6=CC=CC=C6)(C(C(C5C2(C=C(C1=O)OC7C(C(C(C(O7)CO)O)O)O)C)O)O)C(=O)OC 704.70 unknown via CMAUP database
YadanziosideA 101659157 Click to see CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)CC(C)C)(C(C(C5C2(C=C(C1=O)OC6C(C(C(C(O6)CO)O)O)O)C)O)O)C(=O)OC 684.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6R,7Z,10E,11aR)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 49799780 Click to see 348.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Macedonic acid 193076 Click to see 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(5R,7R,8R,9R,10R,13S,17S)-17-[(2S,3S,5R)-5-[(2S)-3,3-dimethyloxiran-2-yl]-2-methoxyoxolan-3-yl]-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate 10414931 Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC)C6C(O6)(C)C)C)C)(C)C 540.70 unknown via CMAUP database
[(5R,7R,8R,9R,10S,11R,13S,17S)-17-[(2S,3S,5R)-5-[(1S)-1,2-dihydroxy-2-methylpropyl]-2-methoxyoxolan-3-yl]-11-hydroxy-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-yl] acetate 71544782 Click to see 574.70 unknown via CMAUP database
1,2-Dihydrobruceajavanin A 10076750 Click to see CC(=O)OC1CC2C(C(=O)CCC2(C3C1(C4=CCC(C4(CC3)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C)C)(C)C 570.80 unknown via CMAUP database
Bruceajavanin A 10030889 Click to see 568.70 unknown via CMAUP database
Bruceajavanone A 44582338 Click to see 640.80 unknown via CMAUP database
Bruceajavanone A 7-Acetate 44582339 Click to see CCCCCC(=O)OC1CC2(C(CC=C2C3(C1C4(C=CC(=O)C(C4CC3OC(=O)C)(C)C)C)C)C5CC(OC5OC(=O)C)C6C(O6)(C)C)C 682.90 unknown via CMAUP database
Bruceajavanone B 44582340 Click to see 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
6-Deoxocastasterone 13870433 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CCC4C3(CC(C(C4)O)O)C)C)O)O 450.70 unknown https://doi.org/10.1016/S0031-9422(00)83445-7
Castasterone 133534 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 464.70 unknown https://doi.org/10.1271/BBB1961.47.655
https://doi.org/10.1016/S0031-9422(00)83445-7
https://doi.org/10.1016/S0021-9673(01)93583-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Brassinolides and derivatives
Brassinolide 115196 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 480.70 unknown https://doi.org/10.1016/S0031-9422(00)83445-7
https://doi.org/10.1016/S0021-9673(01)93583-6
https://doi.org/10.1271/BBB1961.47.655
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4S,5S)-2-[[(3S,8S,9S,10R,13S,14S,17S)-17-[(1R)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 101916318 Click to see 450.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
2-[(1R,2S,3R,6R,8S,9S,10R,11R,12S,13S)-11,12-dihydroxy-13-methoxycarbonyl-8-[(2S)-1-methoxy-1-oxopropan-2-yl]-9-methyl-3-(3-methylbut-2-enoyloxy)-4-oxo-5,14-dioxatetracyclo[8.5.0.01,6.02,13]pentadecan-9-yl]acetic acid 70692363 Click to see 568.60 unknown via CMAUP database
Javanic Acid A 70694422 Click to see CC(C1CC2C34COC(C3C(C(=O)O2)OC(=O)C=C(C)C)(C(C(C4C1(C)CC(=O)O)O)O)C(=O)OC)C(=O)O 554.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(2R,3R,4R,5R)-4-hydroxy-3,5-bis[(3,4,5-trihydroxybenzoyl)oxy]-4-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxolan-2-yl]methyl 3,4,5-trihydroxybenzoate 163019436 Click to see 788.60 unknown https://doi.org/10.1248/CPB.32.483
1,2',3,5-Tetra-O-galloylhamamelofuranose 131752622 Click to see 788.60 unknown https://doi.org/10.1248/CPB.32.483
Bruceanic Acid E 70681802 Click to see 524.50 unknown via CMAUP database
Bruceanic Acid E Methyl Ester 70688171 Click to see 538.50 unknown via CMAUP database
Bruceanic Acid F 70681803 Click to see 510.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines / Methoxypyrazines
Nocazine B 56600877 Click to see 348.40 unknown https://doi.org/10.1248/CPB.44.2236
> Organoheterocyclic compounds / Furopyrans
(1S,2R,3R,4S,6R,7R,10R,11R,12R)-2,6,11,12-tetrahydroxy-4,10-dimethyl-4-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-9,14-dioxatetracyclo[8.4.0.03,7.07,11]tetradecan-13-one 10453339 Click to see 396.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Ethoxycarbonyl-2-quinolone 160782 Click to see 217.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavone 10680 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 222.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/BF02976372
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Luteolin-7-O-galactoside 5488493 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Thevetiaflavone 5315202 Click to see COC1=CC(=CC2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose 73178 Click to see 788.60 unknown https://doi.org/10.1248/CPB.44.2236
1,2,3,6-Tetragalloyl-beta-D-glucopyranose 5153644 Click to see 788.60 unknown https://doi.org/10.1248/CPB.44.2236
> Phenylpropanoids and polyketides / Tannins / Complex tannins
(1S,2S,20S,42S,46R)-46-[(3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 101676951 Click to see 1206.90 unknown https://doi.org/10.1248/CPB.35.602
Acutissimin A 16132408 Click to see C1C(C(OC2=C1C(=CC(=C2C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1206.90 unknown https://doi.org/10.1248/CPB.35.602
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1R,2R,20R,37R,45S,46R,52S)-7,8,9,12,13,14,25,26,27,30,31,32,35,40,41-pentadecahydroxy-4,17,22,36,48,51-hexaoxo-3,18,21,38,47,50-hexaoxaundecacyclo[27.17.3.334,46.02,20.05,10.011,16.023,28.033,49.037,45.039,44.037,52]dopentaconta-5,7,9,11,13,15,23,25,27,29(49),30,32,34,39(44),40,42-hexadecaene-43-carboxylic acid 163195188 Click to see C1C2C(C3C4C5C6=C(C(=C(C=C6C(=O)O)O)O)OC57C(C(=C(C7=O)O)C8=C(C(=C(C(=C8C(=O)O3)C9=C(C(=C(C=C9C(=O)O2)O)O)O)O)O)O)C(=O)O4)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1056.70 unknown https://doi.org/10.1248/CPB.45.1751
(1R,2R,20R,37R,53S,54S,60S)-7,8,9,12,13,14,25,26,27,30,31,32,35,40,46,47-hexadecahydroxy-3,18,21,38,49,55,58,62-octaoxatetradecacyclo[27.25.3.334,54.241,44.02,20.05,10.011,16.023,28.033,57.037,53.039,52.042,51.043,48.037,60]dohexaconta-5,7,9,11,13,15,23,25,27,29(57),30,32,34,39(52),40,42(51),43(48),44,46-nonadecaene-4,17,22,36,50,56,59,61-octone 163020885 Click to see C1C2C(C3C4C5C6=C(C(=C7C8=C6C(=O)OC9=C8C(=CC(=C9O)O)C(=O)O7)O)OC55C(C(=C(C5=O)O)C5=C(C(=C(C(=C5C(=O)O3)C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O)O)C(=O)O4)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1188.80 unknown https://doi.org/10.1248/CPB.45.1751
(1R,2R,20R,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-hexadecahydroxy-15-[(1R,2R,20R,42R,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaen-46-yl]-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11(16),12,14,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 163192175 Click to see 1851.20 unknown https://doi.org/10.1248/CPB.44.2236
(1R,2R,20R,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-hexadecahydroxy-15-[(1R,2R,20R,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaen-46-yl]-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11(16),12,14,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 101998420 Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)C8=C(C(=C(C9=C8C(=O)OCC2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C4=C(C(=C(C(=C4C(=O)O3)C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C29)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1851.20 unknown https://doi.org/10.1248/CPB.44.2236
(1R,2R,20S,42S,46R)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-46-(6,7,13,14-tetrahydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaen-5-yl)-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 163185565 Click to see 1218.80 unknown https://doi.org/10.1248/CPB.45.1751
(1S,2S,24R,25R,29S)-7,8,9,12,13,14,17,18,19,25,29-undecahydroxy-24-(hydroxymethyl)-3,23,26-trioxahexacyclo[13.10.3.12,6.05,10.011,28.016,21]nonacosa-5(10),6,8,11,13,15(28),16,18,20-nonaene-4,22,27-trione 102505445 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C5=C6C(=C(C(=C5O)O)O)C(C(C(C(C(OC2=O)CO)O)OC4=O)OC6=O)O 632.40 unknown https://doi.org/10.1248/CPB.44.2236
1-Epi-castalagin 12302512 Click to see 934.60 unknown https://doi.org/10.1248/CPB.44.2236
3,4,5-trihydroxy-2-[(1R,2R,20S,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaen-46-yl]benzoic acid 163187061 Click to see 1086.70 unknown https://doi.org/10.1248/CPB.45.1751
5-[(2R,3S,3aR,9bR)-2-[(1R)-1,2-dihydroxyethyl]-3,7,8,9-tetrahydroxy-5-oxo-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-6-yl]-6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione 10793860 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C6C(=C(C(=C5O)O)O)C7C(C(C(O7)C(CO)O)O)OC6=O)O)O)OC2=O 614.40 unknown https://doi.org/10.1248/CPB.44.2236
5-[(2R,3S,4S,4aR,10bR)-3,4,8,9,10-pentahydroxy-2-(hydroxymethyl)-6-oxo-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-7-yl]-6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione 10770082 Click to see 614.40 unknown https://doi.org/10.1248/CPB.44.2236
6,7,13,14-tetrahydroxy-5-[5,6,7-trihydroxy-1-oxo-3-[(1S,2R,3R)-1,2,3,4-tetrahydroxybutyl]isochromen-8-yl]-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione 10675279 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C(C(=C(C6=C5C(=O)OC(=C6)C(C(C(CO)O)O)O)O)O)O)O)O)OC2=O 614.40 unknown https://doi.org/10.1248/CPB.44.2236
7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-Hexadecahydroxy-15-(7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-4,17,22,40,44-pentaoxo-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaen-46-yl)-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11(16),12,14,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 72679636 Click to see 1851.20 unknown https://doi.org/10.1248/CPB.44.2236
Castacrenin A 85270241 Click to see 614.40 unknown https://doi.org/10.1248/CPB.44.2236
Castacrenin B 85262147 Click to see 614.40 unknown https://doi.org/10.1248/CPB.44.2236
Castacrenin C 85228592 Click to see 614.40 unknown https://doi.org/10.1248/CPB.44.2236
Castacrenin D 131751205 Click to see 1086.70 unknown https://doi.org/10.1248/CPB.45.1751
Castacrenin E 131751206 Click to see 1056.70 unknown https://doi.org/10.1248/CPB.45.1751
Castacrenin F 131751203 Click to see 1218.80 unknown https://doi.org/10.1248/CPB.45.1751
Castacrenin G 22834921 Click to see 1188.80 unknown https://doi.org/10.1248/CPB.45.1751
Castalagin 12302513 Click to see 934.60 unknown https://doi.org/10.1248/CPB.45.1751
https://doi.org/10.1248/CPB.44.2236
Castalin 99973 Click to see 632.40 unknown https://doi.org/10.1248/CPB.44.2236
CID 5458626 5458626 Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 934.60 unknown https://doi.org/10.1248/CPB.44.2236
https://doi.org/10.1248/CPB.45.1751
Vescalagin 168165 Click to see 934.60 unknown https://doi.org/10.1248/CPB.45.1751
https://doi.org/10.1248/CPB.44.2236
Vescalin 15698968 Click to see 632.40 unknown https://doi.org/10.1248/CPB.44.2236

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